Reprogramming mouse ear mesenchymal stem cells (EMSC) expressing the Dlk1-Dio3 imprinted gene cluster  

作　　者：Ru Gao Jong S. Rim Karen L. Strickler Christian W. Barnes Lettie L. Harkins Jaroslaw Staszkiewicz Jeffery M. Gimble Barbara Gawronska-Kozak Gregory H. Leno Kenneth J. Eilertsen 

机构地区：[1]Department of Anatomy & Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, USA [2]Institute of Animal Reproduction and Food Research of Polish Academy of Sciences, Olsztyn, Poland [3]NuPotential, Inc., Baton Rouge, USA [4]Stem Cell Biology Laboratory, Pennington Biomedical Research Center, Baton Rouge, USA

出　　处：《Stem Cell Discovery》2013年第1期64-71,共8页干细胞探索（英文）

摘　　要：The identification of a single, early marker for full developmental potential of induced pluripotent stem (iPS) cells has proven elusive. Recently, however, activation of the imprinted gene cluster, Dlk1-Dio3 has emerged as a viable candidate in the mouse. To explore the relationship between Dlk1-Dio3 expression and developmental potential more fully, we used murine ear mesenchymal stem cells (mEMSC) for iPS cell induction. Mouse EMSC are easily obtained and share functional characteristics with embryonic stem (ES) cells and therefore, may be a reliable non-embryonic source for iPS cell production. We report that mEMSC express high levels of Gtl2, a maternally expressed gene within the Dlk1-Dio3 imprinted cluster. Moreover, mEMSC produce Gtl2 expressing (Gtl2on) iPSC clones that share functional characteristics with ES cell clones. The production of Gtl2on iPS cell clones from mEMSC provides a new model with which to investigate the regulation of Dlk1-Dio3 cluster activity during direct cell reprogramming.The identification of a single, early marker for full developmental potential of induced pluripotent stem (iPS) cells has proven elusive. Recently, however, activation of the imprinted gene cluster, Dlk1-Dio3 has emerged as a viable candidate in the mouse. To explore the relationship between Dlk1-Dio3 expression and developmental potential more fully, we used murine ear mesenchymal stem cells (mEMSC) for iPS cell induction. Mouse EMSC are easily obtained and share functional characteristics with embryonic stem (ES) cells and therefore, may be a reliable non-embryonic source for iPS cell production. We report that mEMSC express high levels of Gtl2, a maternally expressed gene within the Dlk1-Dio3 imprinted cluster. Moreover, mEMSC produce Gtl2 expressing (Gtl2on) iPSC clones that share functional characteristics with ES cell clones. The production of Gtl2on iPS cell clones from mEMSC provides a new model with which to investigate the regulation of Dlk1-Dio3 cluster activity during direct cell reprogramming.

关 键 词：IPSCS REPROGRAMMING PLURIPOTENT Stem Cell 

分 类 号：R73[医药卫生—肿瘤]